Engström P E, Norhagen G, Bottaro A, Carbonara A O, Lefranc G, Steinitz M, Söder P O, Smith C I, Hammarström L
Department of Clinical Immunology, Karolinska Institute, Huddinge Hospital, Sweden.
J Immunol. 1990 Jul 1;145(1):109-16.
To analyze the subclass restriction of Ag-specific IgA, sera and saliva from healthy blood donors and from IgA class or subclass deficient individuals were studied. The latter included donors with or without C alpha 1 or C alpha 2 gene deletions. Monoclonal human IgA1 and a genetically engineered IgA2 antibody, normal human serum and colostrum IgA were used as standards to estimate serum and saliva levels of Ag-specific antibodies. In normal individuals, there was a strong IgA1 preference of naturally acquired antibodies in serum against both polysaccharide Ag (PPS 6A, PPS 23, pneumococcal C-polysaccharide, and LPS from Escherichia coli) and protein Ag (Staphylococcus aureus alpha-toxin and HSV). Specific IgA2 in serum against the tested Ag were frequently not measurable. In contrast, most of the individuals with homozygous C alpha 1 gene deletions displayed substantial amounts of specific IgA2 against protein as well as polysaccharide Ag. The median levels of specific IgA in serum against protein Ag were approximately one-third as compared to normal individuals and one-fifth, or less, against polysaccharide Ag. Normal serum levels of IgA against the tested Ag, restricted to the IgA1 subclass, were noted in two individuals with IgA2 deficiency, one of whom carried a homozygous C alpha 2 gene deletion. Median values of specific IgA, against the tested Ag S. aureus alpha-toxin, HSV, and pneumococcal C-poly-saccharide, from normal healthy donors were approximately four to eight times higher in serum as compared to saliva. Individuals with homozygous C alpha 1 gene deletions displayed increased levels of the various specific IgA2 antibodies in saliva. In conclusion, the individuals with homozygous C alpha 1 gene deletions displayed decreased median levels of specific IgA antibodies in serum despite normal levels of total IgA. Normal levels of both specific IgA and total IgA in saliva were found.
为分析抗原特异性IgA的亚类限制,对健康献血者以及IgA类或亚类缺陷个体的血清和唾液进行了研究。后者包括存在或不存在Cα1或Cα2基因缺失的献血者。使用单克隆人IgA1、一种基因工程IgA2抗体、正常人血清和初乳IgA作为标准,以估计抗原特异性抗体的血清和唾液水平。在正常个体中,血清中天然获得的针对多糖抗原(PPS 6A、PPS 23、肺炎球菌C多糖和大肠杆菌脂多糖)和蛋白质抗原(金黄色葡萄球菌α毒素和单纯疱疹病毒)的抗体强烈偏向IgA1。血清中针对所测试抗原的特异性IgA2通常无法检测到。相比之下,大多数纯合Cα1基因缺失的个体表现出大量针对蛋白质以及多糖抗原的特异性IgA2。血清中针对蛋白质抗原的特异性IgA的中位数水平约为正常个体的三分之一,针对多糖抗原的则为五分之一或更低。在两名IgA2缺陷个体中观察到正常血清水平的针对所测试抗原的IgA,且仅限于IgA1亚类,其中一人携带纯合Cα2基因缺失。正常健康献血者针对所测试抗原金黄色葡萄球菌α毒素、单纯疱疹病毒和肺炎球菌C多糖的特异性IgA的中位数在血清中比在唾液中高约四至八倍。纯合Cα1基因缺失的个体唾液中各种特异性IgA2抗体水平升高。总之,纯合Cα1基因缺失的个体血清中特异性IgA抗体的中位数水平降低,尽管总IgA水平正常。在唾液中发现了特异性IgA和总IgA的正常水平。